HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1889010Generated: November 1, 2026
Triethylamine → 4-[(3-Chloro-4-fluoro-2-methylphenyl)carbonyl]-2-piperazinone
https://huagongshe.com/reaction/1889010
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Piperazin-2-one | HCID 231360 | — |
| Reactant | 3-Chloro-4-fluoro-2-methylbenzoyl chloride | HCID 86666739 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-[(3-Chloro-4-fluoro-2-methylphenyl)carbonyl]-2-piperazinone | HCID 66599262 | — |
Reaction Steps
2-piperazinone (0.350 g, 3.5 mmol, commercially available from e.g. Sigma-Aldrich) was dissolved in dichloromethane (DCM) (15 mL), and to this was added triethylamine (0.585 mL, 4.20 mmol). The solution was then cooled to 0° C. before 3-chloro-4-fluoro-2-methylbenzoyl chloride (I58) (0.797 g, 3.85 mmol) in Dichloromethane (DCM) (5 mL) was added dropwise. The solution was stirred, under argon, for 30 minutes before the solvent was evaporated in vacuo. The remaining residue was then re-dissolved in DCM (50 mL) and washed with water (20 mL), a saturated solution of sodium bicarbonate (20 mL) and brine (20 mL). The organic phase was then dried over anhydrous sodium sulphate, which was then filtered off and the solvent was evaporated in vacuo. The remaining solid was then stirred in hexane (30 mL) at 55° C. for 30 minutes, before being filtered to yield the product in 0.843 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08501946B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-5289b1b5414349dfa137415ef4d2b324 |
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| Source note | uspto-grants-2013_08 |
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